N-Carbobenzoxyglycine 4-Nitrophenyl Ester

98%

Reagent Code: #217757
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CAS Number 1738-86-9

science Other reagents with same CAS 1738-86-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.3 g/mol
Formula C₁₆H₁₄N₂O₆
badge Registry Numbers
MDL Number MFCD00024663
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an active ester in peptide synthesis, facilitating the coupling of amino acids by enhancing reactivity toward nucleophiles like amines. Its 4-nitrophenyl group acts as a good leaving group, promoting efficient amide bond formation under mild conditions. Commonly employed in solution-phase peptide assembly where selective protection and activation are required. The carbobenzoxy (Cbz) group provides temporary N-protection that can be removed selectively via hydrogenolysis, allowing stepwise chain elongation. Also useful in the preparation of peptide derivatives for biochemical and pharmaceutical research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿1,020.00
N-Carbobenzoxyglycine 4-Nitrophenyl Ester
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Used as an active ester in peptide synthesis, facilitating the coupling of amino acids by enhancing reactivity toward nucleophiles like amines. Its 4-nitrophenyl group acts as a good leaving group, promoting efficient amide bond formation under mild conditions. Commonly employed in solution-phase peptide assembly where selective protection and activation are required. The carbobenzoxy (Cbz) group provides temporary N-protection that can be removed selectively via hydrogenolysis, allowing stepwise chain e

Used as an active ester in peptide synthesis, facilitating the coupling of amino acids by enhancing reactivity toward nucleophiles like amines. Its 4-nitrophenyl group acts as a good leaving group, promoting efficient amide bond formation under mild conditions. Commonly employed in solution-phase peptide assembly where selective protection and activation are required. The carbobenzoxy (Cbz) group provides temporary N-protection that can be removed selectively via hydrogenolysis, allowing stepwise chain elongation. Also useful in the preparation of peptide derivatives for biochemical and pharmaceutical research.

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